Clinical Trials Directory

Trials / Completed

CompletedNCT04657874

Bromelain and Escin in the Reduction of Postoperative Sequelae in Periodontal and Implant Surgery

Association Between Bromelain and Escin in the Reduction of Postoperative Sequelae in Periodontal and Implant Surgery: Randomized Clinical Trial, Placebo-controlled, Double-blind

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
University of L'Aquila · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Accepted

Summary

A randomized clinical trial will be performed in parallel, placebo controlled, triple-blind to evaluate the effectiveness of the association Bromelina and Horse-chestnut (titrated in escin) (Noflogo®, Mavenpharma s.r.l., Rome, Italy) in the management of post trauma-surgery following surgery periodontal and implant surgery.

Detailed description

At least 50 volunteers between the ages of 18 and 50, will be enlisted, with the need to perform one of the interventions described above and that fall within the criteria of inclusion. The study will be carried out in accordance with the Helsinki Declaration on In Vivo Studies and will be initiated with the approval of the Internal Review Board of the University of L'Aquila. The protocol follows the guidelines of the CONSORT Statement for parallel studies and will be recorded on the data base clinicaltrials.gov.

Conditions

Interventions

TypeNameDescription
OTHERBromelains and Escin Oral TabletSupportive care after oral surgery
OTHERPlaceboOral tablet without the active principle

Timeline

Start date
2020-12-01
Primary completion
2021-05-15
Completion
2021-05-27
First posted
2020-12-08
Last updated
2021-09-13

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT04657874. Inclusion in this directory is not an endorsement.